The Waiting Room Revolution

May 14 2024 56

The Waiting Room Revolution Podcast artwork

This podcast can help anyone dealing with serious illness. Over the years, we have cared for and interviewed thousands of patients and families who tell us they felt overwhelmed and ‘in the dark’ during their illness journey. Yet we sometimes heard stories where individuals felt prepared, in control and ‘in the know.’ What was the difference between these experiences? The answer is the 7 keys. Join your hosts Dr. Samantha Winemaker, palliative care doctor, and Dr. Hsien Seow, health care researcher, as they share real-life stories to explain the 7 keys to being hopeful and prepared when facing serious illness. For more information visit: waitingroomrevolution.com Our theme song is Maypole by Ketsa.

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S8: Episode 90: Lisa Levin

May 14 2024 49 mins

This episode features our conversation wtih Lisa Levin, CEO of Advantage Ontario. We chat about how Advantage advocates for seniors quality of life, housing policy that promotes aging in place and what other countries are doing to innovate aging. Learn more about Advantage Ontario here: https://www.advantageontario.ca/ For more information visit: www.waitingroomrevolution.com Our t

S8: Episode 89: Amy Coupal

May 07 2024 47 mins

Happy Caregivers Month! This episode features our conversation with Amy Coupal, the CEO of the Ontario Caregiver Organization. We chat about the services and resources OCO offers, Amy's own caregiving experience and the essential role caregivers have within the healthcare system. Learn more about the Ontario Caregiver Organization here: https://ontariocaregiver.ca Our theme song is

S8: Episode 88: Kelly Clark & Eliza Munro

Apr 30 2024 49 mins

This episode features our conversation with Eliza Munro and Kelly Clark, who are palliative care educators and consultants on IPEPA. IPEPA stands for Indigenous Program of Experience in the Palliative Approach, which is a grass roots approach to breaking down barriers to palliative care for Aboriginal and Torres Strait Islander peoples across Australia. We chat about the important

S8: Episode 87: Daniel Nowoselski

Apr 23 2024 43 mins

This episode features our conversation with Daniel Nowoselski, Advocacy Manager for Hospice Palliative Care at the Canadian Cancer Society. We discuss being a lobbyist for the palliative care community, policy issues and challenges in the health care system that the Canadian Cancer Society are trying to address, where his passion for palliative care stems from, MAID and what brings

S8: Episode 86: Dr. Kerrie Noonan

Apr 16 2024 49 mins

This episode features our conversation with Dr. Kerrie Noonan, clinician psychologist, social researcher, founder and innovator. We talk about death and grief literacy in Australia and around the world, what it is and why it is important and how it really is a community endeavor. Learn more about Kerries work here: https://www.deathliteracy.institute/ Our theme song is Maypole by K

S8: Episode 85: Dr. Red Hoffman

Apr 09 2024 43 mins

This episode features Dr. Red Hoffman, a trauma surgeon who is board certified in hospice and palliative medicine from Asheville, North Carolina. We talk about her upcoming TEDTalk, her life experiences and how she got to where she is now and experiencing emotions as a surgeon alongside caring for your patients. Learn more about Reds work here: https://redhoffmanmd.com/ For more in

S8: Episode 84: Hon. Lisa Raitt

Apr 02 2024 37 mins

This episode features the Hon. Lisa Raitt, former Cabinet Minister and Member of Parliament from 2008 to 2019 and caregiver to her husband Bruce. Bruce was diagnosed with young onset Alzheimer's disease during the pandemic. We talk about their experience with diagnosis, how the seven keys can be used for caregivers and what policies can help caregivers along an illness journey. For

S7: Episode 83: Dr. Kimberly Acquaviva

Dec 12 2023 47 mins

This episode features our conversation with Dr. Kimberly Acquaviva, a professor at the University of Virginias School of Nursing. Kimberly is the author of The Handbook of LGBTQIA-Inclusive Hospice & Palliative Care. We discuss her very personal story of losing her wife Kathy to ovarian cancer and how that shaped her advocacy and how we can provide person centred, inclusive car

S7: Episode 82: Laura Watts

Dec 05 2023 40 mins

In this episode, we chat with Laura Watts: Founder and CEO of CanAge, author, laywer and advocate. She is also an Assistant Professor at University of Toronto where she teaches Law and Aging. In this episode, we discuss CanAge, advocacy in senior patients and families at the policy and individual level, motivation behind her book and aging well around the world. For more informatio

S7: Episode 81: Clare Fuller

Nov 28 2023 42 mins

This episode features our conversation with Clare Fuller, a Registered Nurse with a passion for advance care planning. Clare owns Speak for Me a Lasting Power of Attorney consultant service in the UK. She is also the host of the Conversations about Advance Care podcast. We talk about what shes learned from hosting her podcast and some of the tools shes developed to help people plan